H. S. Dafsari Et Al. , "Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia," JOURNAL OF HUMAN GENETICS , vol.64, no.8, pp.803-813, 2019
Dafsari, H. S. Et Al. 2019. Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia. JOURNAL OF HUMAN GENETICS , vol.64, no.8 , 803-813.
Dafsari, H. S., Sprute, R., Wunderlich, G., Daimagueler, H., KARACA EREK, E., Contreras, A., ... Becker, K.(2019). Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia. JOURNAL OF HUMAN GENETICS , vol.64, no.8, 803-813.
Dafsari, Hormos Et Al. "Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia," JOURNAL OF HUMAN GENETICS , vol.64, no.8, 803-813, 2019
Dafsari, Hormos S. Et Al. "Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia." JOURNAL OF HUMAN GENETICS , vol.64, no.8, pp.803-813, 2019
Dafsari, H. S. Et Al. (2019) . "Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia." JOURNAL OF HUMAN GENETICS , vol.64, no.8, pp.803-813.
@article{article, author={Hormos Salimi Dafsari Et Al. }, title={Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia}, journal={JOURNAL OF HUMAN GENETICS}, year=2019, pages={803-813} }